Amino acid transport through the placenta: an experimental and modelling investigation
Amino acid transport through the placenta: an experimental and modelling investigation
批准号:
BB/I011250/1
负责人:
Colin Sibley
金额:
$37.05万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2012
资助国家:
英国
项目状态:
已结题
起止时间:
2012 至 --
中文摘要
而在子宫中,婴儿从胎盘获得生长和发育所需的所有营养。这个器官将母亲血液中的营养物质转移到婴儿的血液中。如果胎盘没有转移足够的营养物质,胎儿将无法充分发育,可能会出生得太小。出生过小的婴儿更有可能在早期和成年时出现健康问题。为了了解婴儿在子宫中生长的正常过程,以及为什么这个过程有时会受到干扰,我们需要充分了解营养物质是如何通过胎盘运输的。了解正常的胎盘功能将使我们能够确定当婴儿发育受损时可能出现的问题,以及在早期阶段如何预防或治疗。在这个项目中,我们将开发一个关于胎盘功能的计算机模型,该模型可以用来更好地了解胎盘是如何正常工作的,以及在艰难的怀孕中胎盘是如何出错的。我们对氨基酸在胎盘中的转移特别感兴趣。这些都是构成肌肉和生命所必需的细胞“机械”的蛋白质的积木。因此,氨基酸是一类重要的营养物质,它们的胎盘转移对于婴儿在子宫中的最佳生长至关重要。在婴儿出生时较小的妊娠中,胎盘氨基酸的转运已被证明低于正常出生体重的婴儿。胎盘氨基酸转运是一个复杂的过程,它依赖于(I)氨基酸转运体--从母体血液中吸收营养并将其释放到胎儿血液中的载体,(Ii)通过胎盘的血液流动,(Iii)胎盘的内部结构,以及(Iv)母体和胎儿血液中以及组成胎盘的细胞内的氨基酸水平。这些因素影响氨基酸转移的方式不能孤立地理解,因为它们之间存在复杂的相互依赖的相互作用。因此,开发这些复杂相互作用的计算机模型将使我们能够研究胎盘作为一个综合系统是如何工作的。我们已经设计了一个简单的模型,它模拟了人体胎盘中氨基酸转运体的功能,可以预测任何时候多达3个氨基酸的转运。我们已经测试了这个模型,将它与我们在出生后立即收集的胎盘中观察到的实验结果进行了比较。这些测试表明,该模型可以令人信服地再现实验数据,但我们现在需要扩展我们的系统,以准确地模拟整个20种氨基酸的同时运输。这样的模型必须包括对胎盘运输的其他影响,如胎盘的内部结构和血流模式。最终,一个经过充分验证的虚拟胎盘氨基酸运输模型将有助于解释正常胎盘的组成部分如何将氨基酸运输到婴儿并维持最佳生长。它将确定影响胎盘氨基酸运输的最重要因素,并将使未来的研究集中在可能产生最大影响的因素上,从而开发有效的策略,确保婴儿在子宫中以最佳状态成长。这些策略可以包括预测母亲的代谢状态可能如何影响胎盘氨基酸运输的算法(例如,在母亲糖尿病、少女怀孕中),并开发个性化干预措施,或使用该模型来确定药物干预的关键目标。最终,我们希望这项工作将有助于开发一个完全成熟的虚拟胎盘,一个不仅能模拟氨基酸运输,而且能模拟所有胎盘功能的虚拟胎盘。
英文摘要
While in the womb the baby obtains all the nutrients it requires for growth and development from the placenta. This organ transfers nutrients from maternal blood to the baby's blood. If the placenta does not transfer enough nutrients, the fetus will not be able to grow adequately and may be born too small. Babies who are born too small are more likely to develop health problems, both in early life and in adulthood. To understand the normal processes by which babies grow in the womb and to understand why this process is sometimes disturbed, we need to fully appreciate how nutrients are transported across the placenta. Understanding normal placental function will allow us to define what might go wrong when growth of the baby becomes impaired and how this might be prevented or treated at an early stage. In this project we will develop a computer model of how the placenta functions which can be used to better understand how the placenta works normally and also how it can go wrong in a difficult pregnancy. We are particularly interested in the placental transfer of amino acids. These are the building blocks of proteins which form muscles and the cellular 'machinery' essential for life. Thus, amino acids are an important class of nutrients, and their placental transfer is essential for optimal growth of the baby in the womb. In pregnancies where the baby was born small, placental amino acid transport has been shown to be lower than in babies of normal birth weight. Placental amino acid transfer is a complex process which is dependent on (i) amino acid transporters - (carriers) which take nutrients from maternal blood and release them into fetal blood, (ii) on blood flow through the placenta, (iii) on the internal structure of the placenta, and (iv) on the levels of amino acids in maternal and fetal blood as well as inside the cells which make up the placenta. The way these factors affect amino acid transfer cannot be understood in isolation as there are complicated interdependent interactions between them. Therefore, developing a computer model of these complex interactions will allow us to study how the placenta works as an integrated system. We have already designed a simple model that simulates the function of amino acid transporters in the human placenta and which can predict the transport of up to 3 amino acids at any one time. We have tested this model by comparing it to what we observe experimentally in placentas collected immediately after birth. These tests show that the model can convincingly reproduce experimental data, but we now need to expand our system to accurately simulate the simultaneous transport of the entire set of 20 amino acids. Such a model must incorporate other influences on placental transport such as the internal structure and blood flow patterns of the placenta. Ultimately, a well validated virtual placental amino acid transport model will help to explain how the components of the normal placenta function to transport amino acids to the baby and sustain optimal growth. It will identify the most important factors which affect placental amino acid transport and will allow future studies to be focused on such factors that are likely to have the greatest impact, leading to the development of effective strategies to ensure babies grow optimally in the womb. These strategies may include algorithms to predict how mothers metabolic state may affect placental amino acid transport (e.g. in maternal diabetes, teenage pregnancy) and to develop personalised interventions or using the model to identify key targets for pharmacological interventions. Ultimately we intend that this work will contribute to the development of a fully-fledged Virtual Placenta, one that does not just model amino acid transport but all the placental functions.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1096/fj.14-267773
发表时间:
2015-06
期刊:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
影响因子:
--
作者:
[Widdows KL, Panitchob N, Crocker IP, Please CP, Hanson MA, Sibley CP, Johnstone ED, Sengers BG, Lewis RM, Glazier JD]
通讯作者:
Glazier JD
DOI:
10.1016/j.jtbi.2014.10.042
发表时间:
2015-01-21
期刊:
JOURNAL OF THEORETICAL BIOLOGY
影响因子:
2
作者:
[Panitchob, N., Widdows, K. L., Crocker, I. P., Hanson, M. A., Johnstone, E. D., Please, C. P., Sibley, C. P., Glazier, J. D., Lewis, R. M., Sengers, B. G.]
通讯作者:
Sengers, B. G.
DOI:
10.1016/j.bbamem.2016.03.028
发表时间:
2016-07
期刊:
Biochimica et biophysica acta
影响因子:
--
作者:
[Panitchob N, Widdows KL, Crocker IP, Johnstone ED, Please CP, Sibley CP, Glazier JD, Lewis RM, Sengers BG]
通讯作者:
Sengers BG
DOI:
10.1152/ajpregu.00405.2015
发表时间:
2016-02-01
期刊:
American journal of physiology. Regulatory, integrative and comparative physiology
影响因子:
--
作者:
[Lofthouse EM, Perazzolo S, Brooks S, Crocker IP, Glazier JD, Johnstone ED, Panitchob N, Sibley CP, Widdows KL, Sengers BG, Lewis RM]
通讯作者:
Lewis RM
Assessment of Potential Therapies for Pre-eclampsia and Fetal Growth Restriction using Murine Models
-
批准号:G0802770/1
-
项目类别:Research Grant
-
资助金额:$261.42万
-
财政年份:2010
-
负责人:Colin Sibley
-
依托单位:
Magnetic Resonance Imaging Biomarkers for Diagnosing Placentas with Abnormal Diffusional Exchange
-
批准号:G0700308/1
-
项目类别:Research Grant
-
资助金额:$29.97万
-
财政年份:2008
-
负责人:Colin Sibley
-
依托单位:
国内基金
海外基金
登录
查看更多内容
棕榈酸Palmitic acid通过靶向JAK-STAT通路促进致病性Th17细胞分化在儿童性系统性红斑狼疮中的作用及机制研究
-
批准号:2026JJ81716
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:唐金玲
-
依托单位:
基于F/IGF1R/PKC ζ 通路研究夏枯草中
Mesonolic acid B抑制RSV感染性肺炎的
作用机制
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2025
-
负责人:唐维
-
依托单位:
Quinic acid通过抑制肠道菌群代谢产物脱氧胆酸调节巨噬细胞M1向M2极化改善动脉粥样硬化的机制研究
-
批准号:2025JJ80556
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:吴鹏翠
-
依托单位:
脂肪酸α-dimorphecolicacid抑制NF-κB信号介导的小胶质细胞炎症缓解多发性硬化的免疫代谢调控机制研究
-
批准号:QN25H310018
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:杨帆
-
依托单位:
巨噬细胞来源代谢物suberic acid抑制蜕膜早衰防治早产的作用机制研究
-
批准号:82401995
-
项目类别:青年科学基金项目
-
资助金额:--
-
批准年份:2024
-
负责人:梅又文
-
依托单位:
巨噬细胞来源代谢物suberic acid抑制蜕膜早衰防治早产的作用机制研究
-
批准号:--
-
项目类别:青年科学基金项目
-
资助金额:--
-
批准年份:2024
-
负责人:梅又文
-
依托单位:
基于TNF-α靶点的天然化合物Roburic acid防治类风湿性关节炎的分子机制研究
-
批准号:82404638
-
项目类别:青年科学基金项目
-
资助金额:30.00万元
-
批准年份:2024
-
负责人:徐欢欢
-
依托单位:
色氨酸代谢产物Kynurenic Acid在脓毒症肠损伤中的诊断价值及其机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:5.0万元
-
批准年份:2024
-
负责人:陈慧
-
依托单位:
DOT1L抑制剂和Retinoic acid通路激活剂诱导全能性的分子机制
-
批准号:32400656
-
项目类别:青年科学基金项目
-
资助金额:30.00万元
-
批准年份:2024
-
负责人:徐亚星
-
依托单位:
α-酮戊二酸调控ACMSD介导犬尿氨酸通路代谢重编程在年龄相关性听力损失中的作用及机制研究
-
批准号:82371150
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:侯书乐
-
依托单位: